Abstract
Background: Identifying individuals with a higher risk of developing severe coronavirus disease 2019 (COVID-19) outcomes will inform targeted and more intensive clinical monitoring and management. To date, there is mixed evidence regarding the impact of preexisting autoimmune disease (AID) diagnosis and/or immunosuppressant (IS) exposure on developing severe COVID-19 outcomes. Methods: A retrospective cohort of adults diagnosed with COVID-19 was created in the National COVID Cohort Collaborative enclave. Two outcomes, life-threatening disease and hospitalization, were evaluated by using logistic regression models with and without adjustment for demographics and comorbidities. Results: Of the 2 453 799 adults diagnosed with COVID-19, 191 520 (7.81%) had a preexisting AID diagnosis and 278 095 (11.33%) had a preexisting IS exposure. Logistic regression models adjusted for demographics and comorbidities demonstrated that individuals with a preexisting AID (odds ratio [OR], 1.13; 95% confidence interval [CI]: 1.09-1.17; P <. 001), IS exposure (OR, 1.27; 95% CI: 1.24-1.30; P <. 001), or both (OR, 1.35; 95% CI: 1.29-1.40; P <. 001) were more likely to have a life-threatening disease. These results were consistent when hospitalization was evaluated. A sensitivity analysis evaluating specific IS revealed that tumor necrosis factor inhibitors were protective against life-threatening disease (OR, 0.80; 95% CI:. 66-.96; P =. 017) and hospitalization (OR, 0.80; 95% CI:. 73-.89; P <. 001). Conclusions: Patients with preexisting AID, IS exposure, or both are more likely to have a life-threatening disease or hospitalization. These patients may thus require tailored monitoring and preventative measures to minimize negative consequences of COVID-19.
Original language | English |
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Pages (from-to) | 816-826 |
Number of pages | 11 |
Journal | Clinical Infectious Diseases |
Volume | 77 |
Issue number | 6 |
DOIs | |
State | Published - 15 Sep 2023 |
Externally published | Yes |
Keywords
- COVID-19 severity
- N3C retrospective analysis
- TNF inhibitors
- autoimmune disease
- immunosuppressants